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1 ophan binding now allows the formation of an occluded state.
2 rity-dependent structural transitions to the occluded state.
3 ho84 from an open, inward-facing state to an occluded state.
4 site from an outwardly to an inwardly facing occluded state.
5 s of Bor1 have rotated inwards to achieve an occluded state.
6 les of E. coli confirmed the presence of the occluded state.
7 ic conformations, yielding an outward-facing occluded state.
8 y described structures in outward-facing and occluded states.
9 rmational transitions between the closed and occluded states.
10  to promote the structural transition to the occluded state, a step in the transport cycle that is de
11 ubstrate binding and in the formation of the occluded state and to investigate the dynamics of this s
12  binding site to generate a substrate-bound, occluded state, and non-conservative mutation of Tyr130
13 y HDX patterns, revealing that the ion-bound/occluded states are much more stable (rigid) in the OF t
14 substrate appears to stabilize the partially occluded state, as in the two apo simulations either no
15  to 3.6 A resolution, reveals a ligand-bound occluded state for the MFS and provides new insights int
16 formation indicates that a water-impermeable occluded state (glucose and Na(+) in their binding pocke
17 (Aa), a prokaryotic NSS homolog, revealed an occluded state in which one leucine and two Na(+) ions a
18 ne in an apparently open state and one in an occluded state, indicating that SemiSWEETs and SWEETs ar
19                                          The occluded state is formed by rotation of TMs 1 and 2 towa
20                             Furthermore, the occluded state is maintained during cell division and is
21 an extracellular gate that closes to form an occluded state is strongly supported by conformational s
22 ular gate and completes the formation of the occluded state of GluT.
23  molecular dynamics (MD) trajectories of the occluded state of the bacterial leucine transporter LeuT
24 r dynamic simulation showed that a sustained occluded state of the transporter upon binding to co-tra
25        We therefore propose that the outward-occluded state represents a transition intermediate betw
26 galactopyranosides specifically, inducing an occluded state that can open to either side of the membr
27 es transitions between a closed state and an occluded state via an intermediate "open" conformation.
28 e course of MD simulations starting from the occluded state with bound Na(+), but in the absence of s
29 ward-open character and is lower than in the occluded state with bound substrate; however, the Na1 si
30         ATP binding leads to formation of an occluded state with the substrate trapped in the trans-m
31 phate transporter, PiPT, in an inward-facing occluded state, with bound phosphate visible in the memb
32 lodurans, have been resolved in novel inward-occluded states, with the extracellular vestibule closed

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